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Control Release 323, 203224

The cAMP-PKA pathways regulate the activity and expression of the cAMP-response element modulator (CREM) protein family in CD4+ T-cells, linked to effector cytokine expression in psoriasis/PsA and other autoimmune diseases, such as SLE

Water, Butylene Glycol, Niacinamide, 1,2-Hexanediol, Zea Mays (Corn) Starch, Chondrus Crispus Extract, Chlorella Vulgaris Extract, Saccharum Officinarum (Sugarcane) Extract, Centella Asiatica Leaf Extract, Chitosan, Malus Domestica Fruit Cell Culture Extract, Polyacrylate Crosspolymer-6, Betaine, Glucose, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Acetyl Glucosamine, Fructooligosaccharides, Fructose, Glycerin, Pentylene Glycol, Ethylhexylglycerin, Allantoin, Dipropylene Glycol, Adenosine, Glutathione, Madecassoside, Hydroxypropyl Methylcellulose, Hydrogenated Lecithin, Beta-Glucan, Cholesterol, Asiaticoside, Ascorbic Acid, 3-O-Ethyl Ascorbic Acid, Ascorbyl Glucoside, Ceramide NP, Tocopherol, Ferulic Acid, Lactic Acid, Disodium EDTA, Carbomer, Iron Oxides (CI 77491)

The results showed that 5.86, 5.61, and 4.26 times more biotinylation occurred in BME-treated cells than in biotin-treated cells at 1, 5, and 10 M, respectively (Fig

Mouries, J